6 Results for "

2-PCCA

" in MedChemExpress (MCE) Product Catalog:
Products (6)

6 Results for "2-PCCA" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-100013A1
CAS No.: 1609563-71-4
Purity:  98.08%
Target:  

GPR88

Research Areas:  

Neurological Disease

(1R,2R)-2-PCCA hydrochloride is a diastereomer of 2-PCCA, and acts as a potent GPR88 receptor agonist, with an EC50 of 3 nM in cell-free assay, and 603 nM in cell assay.
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Cat. No.: HY-100013C
Purity:  99.63%
Target:  

GPR88

Research Areas:  

Neurological Disease

2-PCCA hydrochloride is a GPR88 receptor agonist, and inhibits GPR88-mediated cAMP production, with an EC50 of 116 nM in HEK293 cells.
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Cat. No.: HY-100013
CAS No.: 1984859-71-3
Target:  

GPR88

Research Areas:  

Neurological Disease

2-PCCA is a racemic form of the GPR88 receptor agonist, and inhibits GPR88-mediated cAMP production, with an EC50 of 116 nM in HEK293 cells.
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Cat. No.: HY-100013B1
CAS No.: 1609563-70-3
Purity:  99.65%
Target:  

GPR88 Drug Isomer

Research Areas:  

Neurological Disease

(1S,2S)-2-PCCA hydrochloride is a less active diastereomer of 2-PCCA. 2-PCCA is a GPR88 receptor agonist, and inhibits GPR88-mediated cAMP production, with an EC50 of 116 nM in HEK293 cells.
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Cat. No.: HY-100013B1R
CAS No.: 1609563-70-3
Research Areas:  

Neurological Disease

(1S,2S)-2-PCCA (hydrochloride) (Standard) is the analytical standard of (1S,2S)-2-PCCA (hydrochloride) (HY-100013B1). This product is intended for research and analytical applications. (1S,2S)-2-PCCA hydrochloride is a less active diastereomer of 2-PCCA. 2-PCCA is a GPR88 receptor agonist, and inhibits GPR88-mediated cAMP production, with an EC50 of 116 nM in HEK293 cells.
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Cat. No.: HY-100013A1R
CAS No.: 1609563-71-4
Research Areas:  

Neurological Disease

(1R,2R)-2-PCCA (hydrochloride) (Standard) is the analytical standard of (1R,2R)-2-PCCA (hydrochloride) (HY-100013A1). This product is intended for research and analytical applications. (1R,2R)-2-PCCA hydrochloride is a diastereomer of 2-PCCA, and acts as a potent GPR88 receptor agonist, with an EC50 of 3 nM in cell-free assay, and 603 nM in cell assay.
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